FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity. - Wikidata - wikimedia - TriplyDB

FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity.

FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity.

http://www.wikidata.org/entity/Q37342489

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Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls Copy number variation at 1q21.1 associated with neuroblastoma Paired-end mapping reveals extensive structural variation in the human genome Microarray resources for genetic and genomic studies in chicken: a review From HLA-B27 to spondyloarthritis: a journey through the ER.Complex and multi-allelic copy number variation in human disease Recent advances in the genetics of autoimmune disease Genomic copy number variants: evidence for association with antibody response to anthrax vaccine adsorbed High basal activity of the PTPN22 gain-of-function variant blunts leukocyte responsiveness negatively affecting IL-10 production in ANCA vasculitis Wegener's granulomatosis: a model of auto-antibodies in mucosal autoimmunity The contribution of genetic variation and infection to the pathogenesis of ANCA-associated systemic vasculitis Simple and versatile molecular method of copy-number measurement using cloned competitors Comprehensive analysis of Copy Number Variation of genes at chromosome 1 and 10 loci associated with late age related macular degeneration Psychomotor retardation with a 1q42.11–q42.12 deletion Population genomics of human gene expression Genome-wide association study of copy number variations (CNVs) with opioid dependence.A genome-wide assessment of the role of untagged copy number variants in type 1 diabetes.Copy number variation in CNP267 region may be associated with hip bone size.Human genes involved in copy number variation: mechanisms of origin, functional effects and implications for disease.A survey of copy-number variation detection tools based on high-throughput sequencing data.Copy number analysis of whole-genome data using BIC-seq2 and its application to detection of cancer susceptibility variants.An Integrated Approach for RNA-seq Data Normalization SeqCNV: a novel method for identification of copy number variations in targeted next-generation sequencing data.Genome-Wide Association Study of Copy Number Variations in Patients with Familial Neurocardiogenic Syncope.Copy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studies.Tyrosine hydroxylase gene: another piece of the genetic puzzle of Parkinson's disease Small deletion variants have stable breakpoints commonly associated with alu elements.Computing power and sample size for case-control association studies with copy number polymorphism: application of mixture-based likelihood ratio test Contrasting genetic association of IL2RA with SLE and ANCA-associated vasculitis Association of FCGR3A and FCGR3B copy number variations with systemic lupus erythematosus and rheumatoid arthritis in Taiwanese patients.Personalized copy number and segmental duplication maps using next-generation sequencing.Quadruplex MAPH: improvement of throughput in high-resolution copy number screening.Copy number variation of FCGR genes in etiopathogenesis of sarcoidosis Copy number variants in genetic susceptibility and severity of systemic lupus erythematosus Contribution of Human FcγRs to Disease with Evidence from Human Polymorphisms and Transgenic Animal Studies Fcgamma receptors: structure, function and role as genetic risk factors in SLE The lupus family registry and repository.Genetic variation of the Fc gamma receptor 3B gene and association with rheumatoid arthritis.Genetic factors predisposing to systemic lupus erythematosus and lupus nephritis.Analysis of copy number variations among diverse cattle breeds.

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FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity.

http://www.wikidata.org/entity/Q37342489

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article científic

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scientific article published on 21 May 2007

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vetenskaplig artikel

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vědecký článek

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name

FCGR3B copy number variation i ...... organ-specific, autoimmunity.

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FCGR3B copy number variation i ...... organ-specific, autoimmunity.

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type

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FCGR3B copy number variation i ...... organ-specific, autoimmunity.

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FCGR3B copy number variation i ...... organ-specific, autoimmunity.

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FCGR3B copy number variation i ...... organ-specific, autoimmunity.

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FCGR3B copy number variation i ...... organ-specific, autoimmunity.

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Nature Genetics

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FCGR3B copy number variation i ...... organ-specific, autoimmunity.

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Adam de Smith

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Alexandra I F Blakemore

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Catherine J Owen

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Charles D Pusey

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Deborah S Cunninghame Graham

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Enrico Petretto

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H Terence Cook

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Joanne M Heward

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Lavanya Kamesh

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Loic Guillevin

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P2860

Fine-scale structural variation of the human genome

Global variation in copy number in the human genome

Detection of large-scale variation in the human genome

Large-scale copy number polymorphism in the human genome

Fcgamma receptors: old friends and new family members

The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility

Fc gamma RIII mediates neutrophil recruitment to immune complexes. a mechanism for neutrophil accumulation in immune-mediated inflammation

Genome architecture, rearrangements and genomic disorders

Pathogenesis of ANCA-associated systemic vasculitis.

Human receptors for immunoglobulin G: key elements in the pathogenesis of rheumatic disease.

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10.1038/NG2046

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6

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39

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Philippe Froguel

Penny J Norsworthy

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2007-05-21T00:00:00Z

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